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干扰素γ诱导的肌炎中补体的协调局部 RNA 过表达。

Coordinated local RNA overexpression of complement induced by interferon gamma in myositis.

机构信息

Muscle Disease Unit, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, 50 South Drive, Room 1141, Building 50, MSC 8024, Bethesda, MD, 20892, USA.

Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Sci Rep. 2023 Feb 4;13(1):2038. doi: 10.1038/s41598-023-28838-z.

Abstract

Complement proteins are deposited in the muscles of patients with myositis. However, the local expression and regulation of complement genes within myositis muscle have not been well characterized. In this study, bulk RNA sequencing (RNAseq) analyses of muscle biopsy specimens revealed that complement genes are locally overexpressed and correlate with markers of myositis disease activity, including the expression of interferon-gamma (IFNγ)-induced genes. Single cell and single nuclei RNAseq analyses showed that most local expression of complement genes occurs in macrophages, fibroblasts, and satellite cells, with each cell type expressing different sets of complement genes. Biopsies from immune-mediated necrotizing myopathy patients, who have the lowest levels of IFNγ-induced genes, also had the lowest complement gene expression levels. Furthermore, data from cultured human cells showed that IFNγ upregulates complement expression in macrophages, fibroblasts, and muscle cells. Taken together, our results suggest that in myositis muscle, IFNγ coordinates the local overexpression of complement genes that occurs in several cell types.

摘要

补体蛋白沉积在肌炎患者的肌肉中。然而,肌炎肌肉中补体基因的局部表达和调节尚未得到很好的描述。在这项研究中,肌肉活检标本的批量 RNA 测序(RNAseq)分析显示,补体基因在局部过度表达,并与肌炎疾病活动的标志物相关,包括干扰素-γ(IFNγ)诱导基因的表达。单细胞和单细胞核 RNAseq 分析表明,补体基因的大部分局部表达发生在巨噬细胞、成纤维细胞和卫星细胞中,每种细胞类型表达不同的补体基因集。免疫介导的坏死性肌病患者的活检标本,IFNγ 诱导基因的水平最低,补体基因的表达水平也最低。此外,来自培养的人细胞的数据表明,IFNγ 上调巨噬细胞、成纤维细胞和肌肉细胞中补体的表达。总之,我们的结果表明,在肌炎肌肉中,IFNγ 协调几种细胞类型中补体基因的局部过度表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45fe/9899209/af295b8bf82d/41598_2023_28838_Fig1_HTML.jpg

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